New Triazoloquinoxaline Ligand and its Polymeric 1D Silver(I) complex Synthesis, Structure, and Antimicrobial activity

Diana, Eliano, Abu-Youssef, Morsy, El-Faham, Ayman, Soliman, Saied M., Albering, Jörg, Sharaf, Mona, Gohar, Yousry M., Gatterer, Karl and Kettle, Sidney F. A. (2018) New Triazoloquinoxaline Ligand and its Polymeric 1D Silver(I) complex Synthesis, Structure, and Antimicrobial activity. New Journal of Chemistry, 42 (9). pp. 7197-7205. ISSN 1144-0546

[img] PDF (Accepted manuscript) - Submitted Version
Restricted to Repository staff only until 27 March 2019.

Download (1394kB) | Request a copy

    Abstract

    The organic ligand 4-Benzyl-1-(N,N-dimethylamino)-[1,2,4]triazolo[4,3a]quinoxaline 1 (L) and its polymeric silver(I) complex, [Ag2L(NO3)2]n (2), have been synthesized and characterized. The organic ligand 1 crystallizes in the triclinic space group P¯1. The unit cell contains two parallel-stacked molecules. The complex [Ag2L(NO3)2]n (2) crystallizes in the monoclinic space group P21/n. The structure contains two different silver(I) ions. Ag(2) is coordinated by three oxygens (involving two nitrate groups) and to a nitrogen of the triazole ring of 1. These ligands form a strongly distorted tetrahedral, nearly planar coordination sphere. Ag(1) has an approximately tetrahedral geometry. It is bonded to one oxygen of a nitrate anion and a nitrogen of two different L; this aspect giving rise to an infinite chain structure. A final bond to Ag(1) involves the carbon of a phenyl group. It is more weakly bonded to the phenyl carbons on either side of this, so that the Ag(1)-phenyl bonding has aspects of an Ag-allyl bond. Ag(1) and Ag(2) participate in bonding to a common nitrate anion and alternate, the two distinct modes of bridging between them lead to a zig-zag chain structure. In addition to spectroscopic studies, the biological activities of the ligand and of the complex were scanned over a wide range of Gram positive and Gram negative flesh- and bone-eating bacteria. The results are discussed in comparison with well-known antibiotics.

    Item Type: Article
    Faculty \ School: Faculty of Science > School of Chemistry
    Related URLs:
    Depositing User: Pure Connector
    Date Deposited: 05 Apr 2018 12:30
    Last Modified: 25 Jul 2018 14:44
    URI: https://ueaeprints.uea.ac.uk/id/eprint/66680
    DOI: 10.1039/C7NJ02886E

    Actions (login required)

    View Item